Department of Pathology, Beijing Friendship Hospital, Capital Medical University, No. 95 Yong-an Road, Xicheng District, Beijing, 100050, China.
Diagn Pathol. 2023 Feb 6;18(1):14. doi: 10.1186/s13000-023-01298-9.
Although epithelioid angiomyolipoma of the kidney has been studied by several groups, the reported prevalence of malignant behavior remains uncertain and there are not yet definitive predictive biomarkers. We evaluated the behavior of renal epithelioid angiomyolipoma in a consecutive series in a single institution and investigated the prognostic value of aberrant p53 expression and TFE3 gene abnormality.
We retrospectively reviewed 14 epithelioid angiomyolipomas, most with pure or close to pure epithelioid components, comprising 12 consecutive cases who had attended our institution and two consultation cases. Fluorescence in situ hybridization with TFE3 break-apart probe was performed on 14 cases. The 14 cases were also labeled for p53 and TFE3 by immunohistochemistry. All cases were followed up.
Three of the epithelioid angiomyolipomas were strongly positive for TFE3 and two had a mutant expression of p53. Although no TFE3 gene rearrangement was found, the two tumors with strong TFE3 expression showed TFE3 gene amplification. Follow-up details were available for seven of the 12 consecutive cases: two of them had developed metastases and died (29%), their mean overall survival was 41 months, and both had mutant p53 expression. The two consultation cases with TFE3 gene amplification developed recurrence/metastasis within 1 year after surgery.
Our series study from a single institution presented the prevalence of malignant behavior in pure epithelioid angiomyolipomas, although the small number of cases with follow-up data greatly reduced the accuracy. p53 may be a prognostic marker for epithelioid angiomyolipoma. Cases with TFE3 gene amplification had poor prognoses.
尽管已有多个研究小组对肾脏上皮样血管平滑肌脂肪瘤进行了研究,但报告的恶性行为发生率仍不确定,也没有明确的预测生物标志物。我们在一家医院的连续病例中评估了肾脏上皮样血管平滑肌脂肪瘤的行为,并研究了异常 p53 表达和 TFE3 基因异常的预后价值。
我们回顾性分析了 14 例上皮样血管平滑肌脂肪瘤,大多数为纯上皮样或接近纯上皮样成分,包括 12 例连续就诊病例和 2 例会诊病例。对 14 例病例进行 TFE3 断裂分离探针的荧光原位杂交。这 14 例病例还通过免疫组化标记 p53 和 TFE3。所有病例均进行了随访。
3 例上皮样血管平滑肌脂肪瘤 TFE3 强阳性,2 例 p53 表达突变。虽然未发现 TFE3 基因重排,但 2 例 TFE3 强表达的肿瘤显示 TFE3 基因扩增。12 例连续病例中有 7 例可获得随访详情:其中 2 例发生转移并死亡(29%),他们的总生存时间平均为 41 个月,且均有突变型 p53 表达。2 例 TFE3 基因扩增的会诊病例在手术后 1 年内复发/转移。
我们的单中心系列研究显示了纯上皮样血管平滑肌脂肪瘤的恶性行为发生率,尽管随访数据的病例数量较少,大大降低了准确性。p53 可能是上皮样血管平滑肌脂肪瘤的预后标志物。TFE3 基因扩增的病例预后不良。